Finasteride
- Product NDC
- 71335-0235
- 11-digit product format
- 713350235
- Labeler code
- 71335
- Product ID
- 71335-0235_026dc9f4-80c4-444e-98dc-c0fec3b3fe67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Finasteride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091643
- Marketing category
- ANDA
- Marketing start
- 2013-11-08
- Marketing end
- 0000-00-00
- Substance
- FINASTERIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0235-1 | 71335023501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0235-1) | 2016-06-23 | 0000-00-00 | No | No | Current |
| 71335-0235-2 | 71335023502 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0235-2) | 2016-06-23 | 0000-00-00 | No | No | Current |
| 71335-0235-3 | 71335023503 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0235-3) | 2016-06-23 | 0000-00-00 | No | No | Current |
| 71335-0235-4 | 71335023504 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0235-4) | 2016-06-23 | 0000-00-00 | No | No | Current |
| 71335-0235-5 | 71335023505 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0235-5) | 2016-06-23 | 0000-00-00 | No | No | Current |